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首页> 外文期刊>鉄と鋼/Journal of the Iron and Steel Institute of Japan. >Simultaneous Determination of Arsenic and Antimony in Steels and Pure Coppers by High Power Nitrogen Microwave Induced Plasma Atomic Emission Spectrometry Coupled with Hydride Generation Technique
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Simultaneous Determination of Arsenic and Antimony in Steels and Pure Coppers by High Power Nitrogen Microwave Induced Plasma Atomic Emission Spectrometry Coupled with Hydride Generation Technique

机译:大功率氮微波等离子体发射光谱法与氢化物发生法同时测定钢和纯铜中的砷和锑。

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The feasibility of an annular-shaped high power nitrogen microwave induced plasma atomic emission spectrometry (N_2-MIP-AES) has been studied for the simultaneous determination of arsenic and antimony in combination with the hydride generation method. Under the optimized experimental conditions, the best attainable detection limits at As I 228.812 and Sb I 231.147 nm lines were 4.13 and 4.50 ng/ml for arsenic and antimony, respectively, with a linear dynamic range of 10 to 10,000 ng/ml in concentrations. The presence of several diverse elements was found to cause more or less a depressing interference by the proposed technique. Of the several pre-reductants examined, thiourea was found to be the most preferable to reduce arsenic and antimony from their pentavalent state to trivalent one prior to hydride generation. Therefore, thiourea was utilized as a pre-reductant for the determination of total arsenic and antimony concentration, i.e., As(III) + As(V) and Sb(III)+Sb(V). When arsenic and antimony in steels were determined simultaneously, a large amount of Fe(III) in the solution caused a severe depressing interference, while the presence of Fe(II) showed little or no significant interference. Of the several interference-releasing agents examined, both thiourea and L-ascorbic acid were found to he the most preferable to reduce Fe(III) to Fe(II). When arsenic and antimony in high purity coppers were determined simultaneously, copper of principal constituent interfered to a great extent. Thiourea was found to reduce the depressing interference from copper, to that any separation procedure of copper matrix was not necessary. The proposed method using thiourea not only as a pre-reductant but also as an interference-releasing agent was applied to the simultaneous determination of low concentrations of arsenic and antimony in carbon steels and high pure coppers. The results obtained by this method were in good agreement with the certified values.
机译:研究了环形大功率氮气微波诱导等离子体原子发射光谱法(N_2-MIP-AES)与氢化物发生法同时测定砷和锑的可行性。在优化的实验条件下,砷和锑的As I 228.812和Sb I 231.147 nm谱线的最佳可获得检出限分别为4.13 ng / ml和4.50 ng / ml,浓度范围为10-10,000 ng / ml的线性动态范围。通过所提出的技术发现了几种不同元素的存在或多或少地引起了令人沮丧的干扰。在所研究的几种预还原剂中,发现硫脲是最优选的,它可以在生成氢化物之前将砷和锑从其五价态还原为三价态。因此,硫脲被用作确定总砷和锑浓度即As(III)+ As(V)和Sb(III)+ Sb(V)的还原剂。同时测定钢中的砷和锑时,溶液中的大量Fe(III)引起严重的压制干扰,而Fe(II)的存在则显示出很少或没有明显的干扰。在所研究的几种减轻干扰的试剂中,硫脲和L-抗坏血酸被认为是将Fe(III)还原为Fe(II)的最优选方法。同时测定高纯度铜中的砷和锑时,主要成分的铜会受到很大程度的干扰。发现硫脲可减少铜的压制干扰,从而无需任何铜基质分离步骤。所提出的方法不仅使用硫脲作为预还原剂,而且还使用了作为干扰消除剂的方法被用于同时测定碳钢和高纯铜中低浓度的砷和锑。通过该方法获得的结果与认证值高度吻合。

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